Kristine Herman has over six years of experience in nonclinical toxicology, including authoring regulatory submission documents, supporting program leads, and providing nonclinical project management support. She has prepared documents for IBs, INDs, and NDAs/BLAs across a variety of therapeutic areas, including oncology, cardiology, orphan diseases, analgesics, metabolic diseases, neurodegenerative disorders, and hormone therapies. Kristine earned a Master's in Pharmacology & Toxicology from Michigan State University.